PubRank

Ah-Ra Ko

Author PubWeight™ 13.65‹?›

Top papers

Rank Title Journal Year PubWeight™‹?›
1 High-dose enzyme replacement therapy attenuates cerebroventriculomegaly in a mouse model of mucopolysaccharidosis type II. J Hum Genet 2013 1.41
2 Phase I/II clinical trial of enzyme replacement therapy with idursulfase beta in patients with mucopolysaccharidosis II (Hunter syndrome). Orphanet J Rare Dis 2013 0.93
3 Therapeutic effects of repetitive transcranial magnetic stimulation in an animal model of Parkinson's disease. Brain Res 2013 0.87
4 Improvement of CNS defects via continuous intrathecal enzyme replacement by osmotic pump in mucopolysaccharidosis type II mice. Am J Med Genet A 2013 0.86
5 Mutations of ACADS gene associated with short-chain acyl-coenzyme A dehydrogenase deficiency. Ann Clin Lab Sci 2011 0.85
6 Identification of signal peptide domain SOST mutations in autosomal dominant craniodiaphyseal dysplasia. Hum Genet 2011 0.84
7 Clinical, biochemical, and genetic analysis of two korean patients with trichorhinophalangeal syndrome type I and growth hormone deficiency. Ann Clin Lab Sci 2012 0.84
8 A polymorphism in the growth hormone receptor is associated with height in children with Prader-Willi syndrome. Am J Med Genet A 2011 0.81
9 A biochemical and physicochemical comparison of two recombinant enzymes used for enzyme replacement therapies of hunter syndrome. Glycoconj J 2014 0.80
10 Five novel mutations of GALNS in Korean patients with mucopolysaccharidosis IVA. Am J Med Genet A 2013 0.80
11 LIN28B polymorphisms are associated with central precocious puberty and early puberty in girls. Korean J Pediatr 2012 0.79
12 Enzyme replacement therapy improves joint motion and outcome of the 12-min walk test in a mucopolysaccharidosis type VI patient previously treated with bone marrow transplantation. Am J Med Genet A 2012 0.78
13 Auditory characteristics and therapeutic effects of enzyme replacement in mouse model of the mucopolysaccharidosis (MPS) II. Am J Med Genet A 2012 0.78
14 A Korean patient with Morquio B disease with a novel c.13_14insA mutation in the GLB1 gene. Ann Clin Lab Sci 2012 0.77
15 A study of the relationship between clinical phenotypes and plasma iduronate-2-sulfatase enzyme activities in Hunter syndrome patients. Korean J Pediatr 2012 0.77
16 Morphological, molecular, and biochemical characterization of astaxanthin-producing green microalga Haematococcus sp. KORDI03 (Haematococcaceae, Chlorophyta) isolated from Korea. J Microbiol Biotechnol 2015 0.76